Skip to content

The implementation of a Tool-Box for sensory aids in geronto-traumatologic patients to reduce the perioperative sensory deficit interval and its effects on the postoperative delir-rate

The implementation of a Tool-Box for sensory aids in geronto-traumatologic patients to reduce the perioperative sensory deficit interval and its effects on the postoperative delir-rate - AnDeBo

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
DRKS
Registry ID
DRKS00022085
Enrollment
150
Registered
2020-07-07
Start date
2020-08-01
Completion date
Unknown
Last updated
2025-04-07

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

F05.0 H91.1

Interventions

Group 1: Historical control group. Auxiliaries are already removed on the ward and the patient is brought to the operation without auxiliaries Group 2: Verum group: Patient retains aids until anaesthe

Sponsors

Else Kröner-Fresenius-Stiftung, Promotionskolleg
Lead Sponsor

Eligibility

Sex/Gender
All
Age
70 Years to No maximum

Inclusion criteria

Inclusion criteria: Gerontotraumatological patients (>70 years) with fracture near the hip and at least 1 sensory aid.

Exclusion criteria

Exclusion criteria: missed inclusion criteria

Design outcomes

Primary

MeasureTime frame
occurrence of postoperative delirium within 72h postoperatively. Measured twice a day using 3D-CAM

Secondary

MeasureTime frame
Premedication Laboratory values (inflammation parameters, kidney values, liver values, metabolism) in regular laboratory controls up to 72h postoperatively Anaesthesia methods (balanced vs. TIVA), Intraoperative arterial intermediate pressure (MAD) Time until surgery Sobering time ASA Classification Anamnestic assessment of the previous illnesses (incl. KHK clarification) Delirious in the prehistory Recovery after the operation

Countries

Germany

Contacts

Public ContactAlexander Ranker

Medizinische hochschule Hannover

ranker.alexander@mh-hannover.de0511532173241

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Feb 4, 2026